霍奇金淋巴瘤出现在两个兄弟姐妹与非典型假胆碱酯酶。

C Wolfla, L Jacobson
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引用次数: 0

摘要

一名21岁的白人男子被诊断为混合细胞霍奇金淋巴瘤,分期剖腹手术。他的家族病史是阳性的兄弟何杰金氏淋巴瘤和非典型假胆碱酯酶。测定血清假胆碱酯酶活性、二布卡因数和氟数,结果显示假胆碱酯酶活性和二布卡因数明显下降,氟数略有下降,与纯合子型E1a型非典型假胆碱酯酶一致。维库溴铵诱导麻醉后,进行分期剖腹手术,无并发症。通过对何杰金氏病和非典型假胆碱酯酶的已知遗传学的讨论,我们得出结论,这两种情况之间的关联非常罕见,但更可能是由于偶然而不是遗传连锁。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hodgkin's lymphoma presenting in two siblings with atypical pseudocholinesterase.

A 21-year-old white man was admitted with a diagnosis of mixed cellularity Hodgkin's lymphoma for staging laparotomy. His family history was positive for a brother who had both Hodgkin's lymphoma and atypical pseudocholinesterase. Serum pseudocholinesterase activity, dibucaine number and fluoride number were obtained, revealing markedly decreased pseudocholinesterase activity and dibucaine number, with an only slightly decreased fluoride number, consistent with homozygous type E1a atypical pseudocholinesterase. After induction of anesthesia using vecuronium, a staging laparotomy was performed without complication. Through a discussion of what is known of the genetics of Hodgkin's disease and atypical pseudocholinesterase, we conclude that the association between the two conditions is very rare but more likely due to chance than to genetic linkage.

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